Senior QC Associate: Precision Analytics & Right-First-Time

MedDeviceJobs; Dublin; On-site; EUR 65,000 - 90,000; Full time

Job summary

MedDeviceJobs in Dublin seeks a QC CAS – Sr Associate to perform analytical testing across Commercial, Stability, Utilities, and raw materials with minimal supervision. The role emphasizes accuracy, compliance, and milestone-driven work within GMP QC laboratories.

The candidate will plan analyses, report trends, validate methods, and contribute to audits and regulatory filings. Extended hours may be required to meet milestones.

Qualifications

• Bachelor’s degree in a Science related field is required.
• 4+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
• Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.

Responsibilities

• Plan and perform analyses with great efficiency and accuracy.
• Plan and perform multiple, complex routine/ non-routine methods and procedures and a large variety of assays.
• Report, evaluate, back-up/archive, trend and approve analytical data.
• Troubleshoot, solve problems and communicate with stakeholders.
• Initiate and/or implement changes in controlled documents.
• Participate in audits, initiatives and projects that may be departmental or organizational in scope.
• Review protocols and perform assay validation and equipment qualification/ verifications when required.
• Introduce new techniques to the lab, including method transfers, reports, validations and protocols.
• May contribute to regulatory filings.
• May conduct lab investigations as necessary.
• Evaluate lab practices for compliance on a continuous basis.
• Approve lab results.
• May interact with outside resources.
• LIMS data coordination of commercial and import testing on site where applicable
• May represent the department/organization on various teams.
• May train others.

Skills

GMP knowledge

QC analysis

Data integrity

Documentation

Troubleshooting

Regulatory compliance

LIMS

Analytical testing

Method validation

Education

Bachelor’s degree in Science

Tools

LIMS

Job description

MedDeviceJobs in Dublin seeks a QC CAS – Sr Associate to perform analytical testing across Commercial, Stability, Utilities, and raw materials with minimal supervision. The role emphasizes accuracy, compliance, and milestone-driven work within GMP QC laboratories.

The candidate will plan analyses, report trends, validate methods, and contribute to audits and regulatory filings. Extended hours may be required to meet milestones.